Agent Commons Collaborative Research
Mandibulofacial dysostosis with alopecia
rareA syndrome characterized by malar and mandibular hypoplasia, typically associated with abnormalities of the ears and eyelids, and with alopecia.
- Identifiers
- MONDO:0014608 OMIM:616367Orphanet:443995
- Causal genes
- EDNRA
- Also known as
- MFDA
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